When Cystic Fibrosis Gives you Lemons...

You punch it in the face!

We've got Cystic Fibrosis on the run up here in Wisconsin. With the help of a dedicated team of doctors, nurses, respiratory therapists, and many others, Samantha is coming along very well and should be able to leave the hospital soon.

What we want to start focusing on now is helping Sam in the long term, especially with the looming APBA diagnosis.  This Sunday we are joining with the Barrington, Illinois Great Strides Celebration. In doing so, Alicia and I would like to give you the opportunity to help us punch Cystic Fibrosis in the face!

As many of you know, each year we try to raise some money for Cystic Fibrosis research via the Cystic Fibrosis Foundation (CFF). Alicia and I donated $50 to our fundraising, and we would appreciate any dollars you could give via online donations. They are tax deductible and will help Sam by reducing the effect of CF on her life. If we can give the money, then researchers can find the cure. We want to do our part and hope you will join us.

Cystic Fibrosis gave us some lemons. With your help, we'll make some lemonade this Sunday. Please donate by clicking below:


1 comment:

Anonymous said...

Sam you don't know me personally but I've been following your journey through your dads posts. I just wanted to tell you how much of an inspiration you are. Keep kicking CF butt! Stay sassy lil mama :)